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In response to who are the 10%? - Non eligibility of cystic fibrosis (CF) patients for highly effective modulator therapies

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Article Cardiac & Cardiovascular Systems

Who are the 10%? - Non eligibility of cystic fibrosis (CF) patients for highly effective modulator therapies

Maya Desai et al.

Summary: Patients from black, Asian and minority ethnic backgrounds are significantly less likely to be eligible for ivacaftor/tezacaftor/elexacaftor based on the current prescribing policy in the UK. These findings highlight the need for effective targeted therapies for cystic fibrosis patients without the F508del mutation.

RESPIRATORY MEDICINE (2022)

Article Pediatrics

Cystic fibrosis patients of minority race and ethnicity less likely eligible for CFTR modulators based on CFTR genotype

Meghan E. McGarry et al.

Summary: This study found that minority groups of cystic fibrosis patients are less likely to be eligible for CFTR modulator therapy, potentially leading to increased disease severity and earlier mortality. This will further contribute to health disparities among people with cystic fibrosis.

PEDIATRIC PULMONOLOGY (2021)

Review Pediatrics

The demographics of adverse outcomes in cystic fibrosis

Meghan E. McGarry et al.

PEDIATRIC PULMONOLOGY (2019)

Article Genetics & Heredity

Hispanic Infants with Cystic Fibrosis Show Low CFTR Mutation Detection Rates in the Illinois Newborn Screening Program

Kimberly Danieli Watts et al.

JOURNAL OF GENETIC COUNSELING (2012)

Editorial Material Pediatrics

Newborn screening for cystic fibrosis: A lesson in public health disparities

Lainie Friedman Ross

JOURNAL OF PEDIATRICS (2008)